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Data updated: Mar 10, 2026

BYQLOVI

CLOBETASOL PROPIONATE
Ophthalmology Approved 2024-03-04
1
Indication
--
Phase 3 Trials
2
Years on Market

Details

Status
Prescription
First Approved
2024-03-04
Routes
OPHTHALMIC
Dosage Forms
SUSPENSION/DROPS

Companies

Active Ingredient: CLOBETASOL PROPIONATE

BYQLOVI Approval History

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What BYQLOVI Treats

2 indications

BYQLOVI is approved for 2 conditions since its original approval in 2024. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Inflammation
  • Pain
Source: FDA Label

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Key Completed Trials

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

BYQLOVI FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

BYQLOVI is indicated for the treatment of post-operative inflammation and pain following ocular surgery. BYQLOVI is a corticosteroid indicated for the treatment of post- operative inflammation and pain following ocular surgery.

BYQLOVI Patents & Exclusivity

Latest Patent: May 2036
Exclusivity: Mar 2027

Patents (2 active)

US11376262 Expires May 9, 2036
US10588913 Expires May 9, 2036

Exclusivity

NP Until Mar 2027
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.